Pistacia integerrima alleviated Bisphenol A induced toxicity through Ubc13/p53 signalling.


Journal

Molecular biology reports
ISSN: 1573-4978
Titre abrégé: Mol Biol Rep
Pays: Netherlands
ID NLM: 0403234

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 24 01 2020
accepted: 02 08 2020
pubmed: 10 8 2020
medline: 26 5 2021
entrez: 10 8 2020
Statut: ppublish

Résumé

Exposure to environmental toxicants such as Bisphenol A (BPA) has raised serious health issues globally particularly in developing countries. It is ubiquitously used in the manufacturing of canned food and feeding bottles. BPA generated reactive oxygen species can lead to several diseases including cardiotoxicity. However, the endpoints stimulated in BPA cardiotoxicity yet need to be investigated. The current study was aimed to investigate the underlying molecular pathways which may contribute in revealing the protective effects of Pistacia integerrima against BPA induced oxidative stress. The dose of 100 µg/kg BW of BPA, 200 mg/kg BW P. integerrima, and 4 mg/kg BW melatonin was administered to Sprague Dawley rats. Present results of western blotting and qRT-PCR showed the increased expression of p53, PUMA and Drp1, while downregulation of Ubc13 in heart tissues of BPA treated group whereas the levels were reversed upon treatment with P. integerrima. The role of BPA in heart tissue apoptosis was further confirmed by the increased level of P-p53, cytochrome C and disrupted cellular architecture whereas the P. integerrima has shown its ameliorative potential by mitigating the adverse effects of BPA. Moreover, the oxidant, antioxidant, lipid, and liver markers profile has also revealed the therapeutic potential of P. integerrima by maintaining the levels in the normal range. However, melatonin has also manifested the normalized expression of apoptotic markers, biochemical markers, and tissue architecture. Conclusively, the data suggest that P. integerrima may be a potential candidate for the treatment of BPA induced toxicity by neutralizing the oxidative stress through Ubc13/p53 pathway.

Identifiants

pubmed: 32770526
doi: 10.1007/s11033-020-05706-x
pii: 10.1007/s11033-020-05706-x
doi:

Substances chimiques

Antioxidants 0
Apoptosis Regulatory Proteins 0
Bbc3 protein, rat 0
Benzhydryl Compounds 0
Blood Glucose 0
Phenols 0
Plant Extracts 0
Reactive Oxygen Species 0
Tp53 protein, rat 0
Tumor Suppressor Protein p53 0
Cytochromes c 9007-43-6
Ube2n protein, rat EC 2.3.2.23
Ubiquitin-Conjugating Enzymes EC 2.3.2.23
Dnm1l protein, rat EC 3.6.5.5
Dynamins EC 3.6.5.5
Melatonin JL5DK93RCL
bisphenol A MLT3645I99

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6545-6559

Subventions

Organisme : Higher Education Commission, Pakistan
ID : NRPU
Organisme : Quaid-i-Azam University
ID : URF

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Auteurs

Ayesha Ishtiaq (A)

Signal Transduction Lab, Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.

Attia Bakhtiar (A)

Signal Transduction Lab, Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.

Erica Silas (E)

Signal Transduction Lab, Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.

Javeria Saeed (J)

Signal Transduction Lab, Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.

Sidra Ajmal (S)

Signal Transduction Lab, Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.

Iram Mushtaq (I)

Signal Transduction Lab, Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.

Tahir Ali (T)

Signal Transduction Lab, Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.

Hussain M Wahedi (HM)

Department of Biological Sciences, National University of Medical Sciences, C/O MH, Rawalpindi, 46000, Pakistan.

Wajiha Khan (W)

Department of Biotechnology, COMSATS University Islamabad, Abbottabad Campus, Abbottabad, Pakistan.

Uzma Khan (U)

Faculty of Biological Sciences, Hazara University, Mansehra, KPK, Pakistan.

Mariam Anees (M)

Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.

Aneesa Sultan (A)

Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.

Iram Murtaza (I)

Signal Transduction Lab, Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan. irambch@qau.edu.pk.

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